iKAR Vita Wadent Dental Hand Instruments (Unsterilized)
Taiwan·Risk Class 1·IVOCLAR VIVADENT AG·Registered Oct 30, 2007 – Oct 30, 2012Cancelled- Analysis ID
- d635f1fd193d60043aec553f04869656
- Customs Code
- DHA04400625902
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- TSENG LIMITED
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
- Registration Date
- Oct 30, 2007
- Expiry Date
- Oct 30, 2012
- Cancellation Date
- Apr 15, 2014
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for iKAR Vita Wadent Dental Hand Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d635f1fd193d60043aec553f04869656 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is TSENG LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IVOCLAR VIVADENT, INC, GEB. BRASSELER GMBH & CO KG;; IVOCLAR VIVADENT AG, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.